Fibrocystic breast disease: Pathophysiology, pathomorphology, clinical picture, and management
The pathophysiology of fibrocystic breast disease is determined by estrogen predominance and progesterone deficiency that result in hyperproliferation of connective tissue (fibrosis), which is followed by facultative epithelial proliferation; the risk of breast cancer is increased twofold to fourfol...
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Veröffentlicht in: | American journal of obstetrics and gynecology 1986-01, Vol.154 (1), p.161-179 |
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description | The pathophysiology of fibrocystic breast disease is determined by estrogen predominance and progesterone deficiency that result in hyperproliferation of connective tissue (fibrosis), which is followed by facultative epithelial proliferation; the risk of breast cancer is increased twofold to fourfold in these patients. The clinical correlate of fibrocystic disease is reflected by breast and axillary pain or tenderness in response to development of fibrocystic plaques, nodularity, macrocysts, and fibrocystic lumps. The disease progresses with advancing premenopausal age and is most pronounced in women during their 40s. Fibrocystic changes regress during the postmenopausal period. Medical treatment of fibrocystic disease is accomplished: (1) by suppression of ovarian estrogen secretion with a low-estrogen oral contraceptive, whereby the action of estrogen on breast tissues is opposed by the oral contraceptive's progestin component (19-nortestosterone derivatives), or (2) by cyclic administration of a progestogen (progesterone, medroxyprogesterone acetate) that modulates the mammary effects of estrogen. These treatment mocalities are equally as effective as or superior to danazol therapy, which entails side effects in the majority of patients. Adjuvant therapy of fibrocystic breast disease with vitamin E is of value in patients with borderline or abnormal lipid profiles (low plasma levels of high-density lipoprotein and high plasma leveis of low-density lipoprotein). With thorough diagnostic evaluation, appropriate medication, and close follow-up, treatment success can be achieved in almost every patient. Needle aspiration biopsy should be performed in patients with macrocysts and whenever clinical, ultrasonic, and/or mammographic examinations are suspicious for carcinoma. Patients at high risk of breast cancer (breast cancer in mother and/or sister) should have clinical examinations at 4- to 6-month intervals and mammography every 1 to 2 years; needle aspiration should be performed when the slightest suspicion arises. Fibrocystic breast disease is not a “harmless nondisease” but a distinct clinical entity that requires treatment to bring about rellef to the patient, to reduce the incidence of breast surgical procedures, and to diminish the risk of breast cancer. |
doi_str_mv | 10.1016/0002-9378(86)90421-7 |
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The clinical correlate of fibrocystic disease is reflected by breast and axillary pain or tenderness in response to development of fibrocystic plaques, nodularity, macrocysts, and fibrocystic lumps. The disease progresses with advancing premenopausal age and is most pronounced in women during their 40s. Fibrocystic changes regress during the postmenopausal period. Medical treatment of fibrocystic disease is accomplished: (1) by suppression of ovarian estrogen secretion with a low-estrogen oral contraceptive, whereby the action of estrogen on breast tissues is opposed by the oral contraceptive's progestin component (19-nortestosterone derivatives), or (2) by cyclic administration of a progestogen (progesterone, medroxyprogesterone acetate) that modulates the mammary effects of estrogen. These treatment mocalities are equally as effective as or superior to danazol therapy, which entails side effects in the majority of patients. Adjuvant therapy of fibrocystic breast disease with vitamin E is of value in patients with borderline or abnormal lipid profiles (low plasma levels of high-density lipoprotein and high plasma leveis of low-density lipoprotein). With thorough diagnostic evaluation, appropriate medication, and close follow-up, treatment success can be achieved in almost every patient. Needle aspiration biopsy should be performed in patients with macrocysts and whenever clinical, ultrasonic, and/or mammographic examinations are suspicious for carcinoma. Patients at high risk of breast cancer (breast cancer in mother and/or sister) should have clinical examinations at 4- to 6-month intervals and mammography every 1 to 2 years; needle aspiration should be performed when the slightest suspicion arises. Fibrocystic breast disease is not a “harmless nondisease” but a distinct clinical entity that requires treatment to bring about rellef to the patient, to reduce the incidence of breast surgical procedures, and to diminish the risk of breast cancer.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/0002-9378(86)90421-7</identifier><identifier>PMID: 3511705</identifier><identifier>CODEN: AJOGAH</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Adenofibroma - pathology ; Adenoma - pathology ; Adult ; Aged ; Biological and medical sciences ; Breast - injuries ; Breast Neoplasms - pathology ; Bromocriptine - therapeutic use ; Contraceptives, Oral, Combined - therapeutic use ; Cysts - pathology ; Danazol - therapeutic use ; Epithelium - pathology ; Estrogens - blood ; Female ; Fibrocystic Breast Disease - etiology ; Fibrocystic Breast Disease - pathology ; Fibrocystic Breast Disease - physiopathology ; Fibrocystic Breast Disease - therapy ; Fibrocystic disease ; Gynecology. Andrology. Obstetrics ; Humans ; Hyperplasia - pathology ; Mammary gland diseases ; Mammography ; management ; Mastectomy ; Medical sciences ; Middle Aged ; Nipples - physiopathology ; Non tumoral diseases ; Norethindrone - therapeutic use ; Papilloma - pathology ; pathobiology ; Population ; Progesterone - blood ; Progestins - therapeutic use ; Prolactin - blood ; Thyroid Hormones - blood ; Ultrasonography ; Vitamin E - therapeutic use ; Xanthines - blood</subject><ispartof>American journal of obstetrics and gynecology, 1986-01, Vol.154 (1), p.161-179</ispartof><rights>1986</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-7039224cfb536d7bb1501f6701f1480db58afdeeadb1872f485f392997deb3603</citedby><cites>FETCH-LOGICAL-c386t-7039224cfb536d7bb1501f6701f1480db58afdeeadb1872f485f392997deb3603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0002-9378(86)90421-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,4010,27904,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8756576$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3511705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vorherr, Helmuth</creatorcontrib><title>Fibrocystic breast disease: Pathophysiology, pathomorphology, clinical picture, and management</title><title>American journal of obstetrics and gynecology</title><addtitle>Am J Obstet Gynecol</addtitle><description>The pathophysiology of fibrocystic breast disease is determined by estrogen predominance and progesterone deficiency that result in hyperproliferation of connective tissue (fibrosis), which is followed by facultative epithelial proliferation; the risk of breast cancer is increased twofold to fourfold in these patients. The clinical correlate of fibrocystic disease is reflected by breast and axillary pain or tenderness in response to development of fibrocystic plaques, nodularity, macrocysts, and fibrocystic lumps. The disease progresses with advancing premenopausal age and is most pronounced in women during their 40s. Fibrocystic changes regress during the postmenopausal period. Medical treatment of fibrocystic disease is accomplished: (1) by suppression of ovarian estrogen secretion with a low-estrogen oral contraceptive, whereby the action of estrogen on breast tissues is opposed by the oral contraceptive's progestin component (19-nortestosterone derivatives), or (2) by cyclic administration of a progestogen (progesterone, medroxyprogesterone acetate) that modulates the mammary effects of estrogen. These treatment mocalities are equally as effective as or superior to danazol therapy, which entails side effects in the majority of patients. Adjuvant therapy of fibrocystic breast disease with vitamin E is of value in patients with borderline or abnormal lipid profiles (low plasma levels of high-density lipoprotein and high plasma leveis of low-density lipoprotein). With thorough diagnostic evaluation, appropriate medication, and close follow-up, treatment success can be achieved in almost every patient. Needle aspiration biopsy should be performed in patients with macrocysts and whenever clinical, ultrasonic, and/or mammographic examinations are suspicious for carcinoma. Patients at high risk of breast cancer (breast cancer in mother and/or sister) should have clinical examinations at 4- to 6-month intervals and mammography every 1 to 2 years; needle aspiration should be performed when the slightest suspicion arises. Fibrocystic breast disease is not a “harmless nondisease” but a distinct clinical entity that requires treatment to bring about rellef to the patient, to reduce the incidence of breast surgical procedures, and to diminish the risk of breast cancer.</description><subject>Adenofibroma - pathology</subject><subject>Adenoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Breast - injuries</subject><subject>Breast Neoplasms - pathology</subject><subject>Bromocriptine - therapeutic use</subject><subject>Contraceptives, Oral, Combined - therapeutic use</subject><subject>Cysts - pathology</subject><subject>Danazol - therapeutic use</subject><subject>Epithelium - pathology</subject><subject>Estrogens - blood</subject><subject>Female</subject><subject>Fibrocystic Breast Disease - etiology</subject><subject>Fibrocystic Breast Disease - pathology</subject><subject>Fibrocystic Breast Disease - physiopathology</subject><subject>Fibrocystic Breast Disease - therapy</subject><subject>Fibrocystic disease</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Hyperplasia - pathology</subject><subject>Mammary gland diseases</subject><subject>Mammography</subject><subject>management</subject><subject>Mastectomy</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nipples - physiopathology</subject><subject>Non tumoral diseases</subject><subject>Norethindrone - therapeutic use</subject><subject>Papilloma - pathology</subject><subject>pathobiology</subject><subject>Population</subject><subject>Progesterone - blood</subject><subject>Progestins - therapeutic use</subject><subject>Prolactin - blood</subject><subject>Thyroid Hormones - blood</subject><subject>Ultrasonography</subject><subject>Vitamin E - therapeutic use</subject><subject>Xanthines - blood</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxTAQhYMoen38A4UuRBSsJn0kqQtBxBcIutCtIY-pN9I2NekV7r839Za7dDPDzJxzEj6EDgm-IJjQS4xxllY546ecnlW4yEjKNtCM4IqllFO-iWZryQ7aDeFrHLMq20bbeUkIw-UMfdxb5Z1ehsHqRHmQYUiMDbHDVfIqh7nr58tgXeM-l-dJPy5a5_v5tNCN7ayWTdJbPSw8nCeyM0krO_kJLXTDPtqqZRPgYOp76P3-7u32MX1-eXi6vXlOdc7pkDKcV1lW6FqVOTVMKVJiUlMWCyk4NqrksjYA0ijCWVYXvKyjo6qYAZVTnO-hk1Vu7933AsIgWhs0NI3swC2CYDGrYpRGYbESau9C8FCL3ttW-qUgWIxYxQhJjMwEp-IPq2DRdjTlL1QLZm2aOMb78XSXIeKovey0DWsZZyUt2fj69UoGkcWPBS-CttBpMNaDHoRx9v9__AKLo5R-</recordid><startdate>198601</startdate><enddate>198601</enddate><creator>Vorherr, Helmuth</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198601</creationdate><title>Fibrocystic breast disease: Pathophysiology, pathomorphology, clinical picture, and management</title><author>Vorherr, Helmuth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-7039224cfb536d7bb1501f6701f1480db58afdeeadb1872f485f392997deb3603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Adenofibroma - pathology</topic><topic>Adenoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Breast - injuries</topic><topic>Breast Neoplasms - pathology</topic><topic>Bromocriptine - therapeutic use</topic><topic>Contraceptives, Oral, Combined - therapeutic use</topic><topic>Cysts - pathology</topic><topic>Danazol - therapeutic use</topic><topic>Epithelium - pathology</topic><topic>Estrogens - blood</topic><topic>Female</topic><topic>Fibrocystic Breast Disease - etiology</topic><topic>Fibrocystic Breast Disease - pathology</topic><topic>Fibrocystic Breast Disease - physiopathology</topic><topic>Fibrocystic Breast Disease - therapy</topic><topic>Fibrocystic disease</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Hyperplasia - pathology</topic><topic>Mammary gland diseases</topic><topic>Mammography</topic><topic>management</topic><topic>Mastectomy</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nipples - physiopathology</topic><topic>Non tumoral diseases</topic><topic>Norethindrone - therapeutic use</topic><topic>Papilloma - pathology</topic><topic>pathobiology</topic><topic>Population</topic><topic>Progesterone - blood</topic><topic>Progestins - therapeutic use</topic><topic>Prolactin - blood</topic><topic>Thyroid Hormones - blood</topic><topic>Ultrasonography</topic><topic>Vitamin E - therapeutic use</topic><topic>Xanthines - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vorherr, Helmuth</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vorherr, Helmuth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fibrocystic breast disease: Pathophysiology, pathomorphology, clinical picture, and management</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>1986-01</date><risdate>1986</risdate><volume>154</volume><issue>1</issue><spage>161</spage><epage>179</epage><pages>161-179</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><coden>AJOGAH</coden><abstract>The pathophysiology of fibrocystic breast disease is determined by estrogen predominance and progesterone deficiency that result in hyperproliferation of connective tissue (fibrosis), which is followed by facultative epithelial proliferation; the risk of breast cancer is increased twofold to fourfold in these patients. The clinical correlate of fibrocystic disease is reflected by breast and axillary pain or tenderness in response to development of fibrocystic plaques, nodularity, macrocysts, and fibrocystic lumps. The disease progresses with advancing premenopausal age and is most pronounced in women during their 40s. Fibrocystic changes regress during the postmenopausal period. Medical treatment of fibrocystic disease is accomplished: (1) by suppression of ovarian estrogen secretion with a low-estrogen oral contraceptive, whereby the action of estrogen on breast tissues is opposed by the oral contraceptive's progestin component (19-nortestosterone derivatives), or (2) by cyclic administration of a progestogen (progesterone, medroxyprogesterone acetate) that modulates the mammary effects of estrogen. These treatment mocalities are equally as effective as or superior to danazol therapy, which entails side effects in the majority of patients. Adjuvant therapy of fibrocystic breast disease with vitamin E is of value in patients with borderline or abnormal lipid profiles (low plasma levels of high-density lipoprotein and high plasma leveis of low-density lipoprotein). With thorough diagnostic evaluation, appropriate medication, and close follow-up, treatment success can be achieved in almost every patient. Needle aspiration biopsy should be performed in patients with macrocysts and whenever clinical, ultrasonic, and/or mammographic examinations are suspicious for carcinoma. Patients at high risk of breast cancer (breast cancer in mother and/or sister) should have clinical examinations at 4- to 6-month intervals and mammography every 1 to 2 years; needle aspiration should be performed when the slightest suspicion arises. Fibrocystic breast disease is not a “harmless nondisease” but a distinct clinical entity that requires treatment to bring about rellef to the patient, to reduce the incidence of breast surgical procedures, and to diminish the risk of breast cancer.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>3511705</pmid><doi>10.1016/0002-9378(86)90421-7</doi><tpages>19</tpages></addata></record> |
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subjects | Adenofibroma - pathology Adenoma - pathology Adult Aged Biological and medical sciences Breast - injuries Breast Neoplasms - pathology Bromocriptine - therapeutic use Contraceptives, Oral, Combined - therapeutic use Cysts - pathology Danazol - therapeutic use Epithelium - pathology Estrogens - blood Female Fibrocystic Breast Disease - etiology Fibrocystic Breast Disease - pathology Fibrocystic Breast Disease - physiopathology Fibrocystic Breast Disease - therapy Fibrocystic disease Gynecology. Andrology. Obstetrics Humans Hyperplasia - pathology Mammary gland diseases Mammography management Mastectomy Medical sciences Middle Aged Nipples - physiopathology Non tumoral diseases Norethindrone - therapeutic use Papilloma - pathology pathobiology Population Progesterone - blood Progestins - therapeutic use Prolactin - blood Thyroid Hormones - blood Ultrasonography Vitamin E - therapeutic use Xanthines - blood |
title | Fibrocystic breast disease: Pathophysiology, pathomorphology, clinical picture, and management |
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